NDC 63776-175 Viatrexx-f Gus

Berberis, Cochlerearia Armor, Echinacea, Ferrum, Hydrastis, Iridium, Lapacho, Lomatium, Lycopodium, Myrrh, Phosporicum Acidum, Propolis, Pulsatilla, Seleneium, Thymus, Zinc

NDC Product Code 63776-175

NDC CODE: 63776-175

Proprietary Name: Viatrexx-f Gus What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Berberis, Cochlerearia Armor, Echinacea, Ferrum, Hydrastis, Iridium, Lapacho, Lomatium, Lycopodium, Myrrh, Phosporicum Acidum, Propolis, Pulsatilla, Seleneium, Thymus, Zinc What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 63776-175-11

Package Description: .5 mL in 1 AMPULE

NDC 63776-175-14

Package Description: 30 mL in 1 BOTTLE

NDC 63776-175-15

Package Description: 50 mL in 1 BOTTLE

NDC 63776-175-16

Package Description: 100 mL in 1 BOTTLE

NDC 63776-175-17

Package Description: 250 mL in 1 BOTTLE

NDC 63776-175-18

Package Description: 500 mL in 1 BOTTLE

NDC 63776-175-19

Package Description: 1000 mL in 1 BOTTLE

NDC Product Information

Viatrexx-f Gus with NDC 63776-175 is a a human over the counter drug product labeled by Viatrexx Bio Incorporated. The generic name of Viatrexx-f Gus is berberis, cochlerearia armor, echinacea, ferrum, hydrastis, iridium, lapacho, lomatium, lycopodium, myrrh, phosporicum acidum, propolis, pulsatilla, seleneium, thymus, zinc. The product's dosage form is spray and is administered via oral; topical form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Viatrexx-f Gus Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Viatrexx Bio Incorporated
Labeler Code: 63776
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-29-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Viatrexx-f Gus Product Label Images

Viatrexx-f Gus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Acidum phosphoricum (12X), berberis 3X, Cochlearia armor 3X, Echinacea (3X), ferrum 12X, Hydrastis (3X), iridium 12X, Lapacho 3X, Lomatium 3X, Lycopodium (12X), Myrrh 3X, Propolis 3X, Pulsatilla 12X, Selenium 12X, Thymus (6X), Zinc (12X).


Viatrexx-F gus is a homeopathic product composed of physiological (low dose and low low dose) natural micro nutrients. These micro particles are designed to nourish the system.


Nutritional support for fungal, mold, bacteria challenges


1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.


Stop use and ask a health care practitioner if symptoms persist for more than 5 days or worsen. If pregnant or breastfeeding, ask a health care practitioner before use.

Inactive Ingredients

20% Alcohol and 80% Water.

Product Availability

Product may be acquired in 0.5, 30 ,50, 100, 250, 500, 1,000 mL bottles.References upon requestTo report SUSPECTED ADVERSE REACTIONS, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatchDistributed by Viatrexx Bio Incorporated Newark, DE, USA, 19713Manufactured by 8046255 Canada Inc Beloeil, Qc, J3G 6S3 Date of last revision March 2019 For Questions and comments [email protected] www.Viatrexx.com

* Please review the disclaimer below.